The effect of minirin® on sleeping and voiding pattern to whom circadian rhythmic changed work-shift nurses

Not Applicable

Recruiting

Conditions: Not Applicable

Registration Number: KCT0001223

Lead Sponsor: Ferring pharmaceuticals Korea

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Female

Target Recruitment: 34

Inclusion Criteria

1) Female nurse at the age of 20 ~ 50 who assigned to the general ward and sifted to the nigh duty
2) A woman without any LUTS
3) A woman who has given written informed consent from voluntarily before any trial related actives

Exclusion Criteria

1) A woman who has history of urinary tract infections within one month.
2) A woman who has been treated with alpha-blocker, anticholinergic, cholinergic, diuretic for more than three months.
3) A woman who is during her menstrual period
4) A woman who is pregnant or is under breast feeding
5) A woman who has history of SIADH
6) A woman who has nocturnal polyuria, hypertention, chronic renal disease, or cardiovascular disease
7) A woman who has habitual or psychotic polydypsia (24 hrs urine output > 40ml/kg)
8) A woman who has history of chronic pelvic pain syndrome.
9) A woman who has history of cancer in abdominal or endopelvis.
10) A woman who treated with pelvic radiation therapy.
11) A woman who received transurethral resection (TUR).
12) A woman diagnosed with interstitial cystitis.
13) A woman who be considered unacceptable by investigator.

Study & Design

Study Type: Interventional Study

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
voiding diary ;OABSS: overactive bladder symptom score;PSQI-K: Pittsburgh Sleep Quality Index Korean;KESS: Korean version of the Epworth Sleepiness Scale

Secondary Outcome Measures